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Tender For srph153041-coronary drug eluting stents with (1) stent on cobalt chromi um alloy or platinum chromium alloy. (2) stent with coating of polymer carrier for active drug ( sirolimus, everolimus or zotarolimus shown to be effective in preven ting neo-intimal hyperplasia) (3) stent diameter should be from 2.5mm to 4mm and len gth of the stent from 12mm to 38 mm. (4) the strut thickness should be 91 micron or less. (5) stent delivery system should be monorail (single operator exchange or ra pid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent desi gn should be open cell type. (8) stent should be approved by dcgi. the copy of dcgi approval should be enclosed in the tender bid. (9) the long term efficacy and safet y of the stent in terms of target vessel revascularisation (tvr) and in-situ thromb osis (ist) should be documented / published in peer reviewed scientific journals.(10) the documents pertaining to the efficacy and safety of the stent should be enclos ed for the brand that is offered in the tender bid (11) the manufacturer/supplier sh ould submit proof of supply of the stent to a major government institute.unit: no. [ warranty period: 30 months after the date of delivery ]
Tender For srph153042- coronary drug eluting stents with (1) stent on cobalt chromi um alloy or platinum chromium alloy. (2) stent with coating of polymer carrier for active drug ( sirolimus, everolimus or zotarolimus shown to be effective in preven ting neo-intimal hyperplasia) (3) stent diameter should be from 2.5mm to 4mm and len gth of the stent should be 12mm to 48mm. (4) the strut thickness should be 91 micron or less. (5) stent delivery system should be monorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent d esign should be open cell type. (8) stent should be approved by dcgi. the copy of dc gi approval should be enclosed in the tender bid. (9) the long term efficacy and saf ety of the stent in terms of target vessel revascularisation (tvr) and in-situ throm bosis (ist) should be documented / published in peer reviewed scientific journals. (10 ) the documents related to the efficacy and safety of the stent should be only for the brand that is offered in the tender bid (11) the manufacturer/supplier should s ubmit proof of supply of the stent to a major government institute. unit:no [ warranty period: 30 months after the date of delivery ]
Tender For srph153042-coronary drug eluting stents with (1) stent on cobalt chromi um alloy or platinum chromium alloy. (2) stent with coating of polymer carrier for active drug ( sirolimus, everolimus or zotarolimus shown to be effective in preven ting neo-intimal hyperplasia) (3) stent diameter should be from 2.5mm to 4mm . the le ngth of the stent should be 12 to 48mm . (4) the strut thickness should be 91 micron or less. (5) stent delivery system should be monorail (single operator exchange or rapid exchange). (6) stent should be compatible with 5fr guiding catheter (7) stent d esign should be open cell type. (8) stent should be approved by dcgi. the copy of dc gi approval should be enclosed in the tender bid / offer. (9) the long term efficacy and safety of the stent, the rates of in-stent restenosis (isr) and in-situ thrombosi s (ist) should be documented / published in peer reviewed scientific journals. (10)the manufacturer/supplier should submit proof of supply of the stent to a major gov ernment institute.bis standards for the drug eluting stent are not available (refe rence : bis catalogue ) unit: no.